NOBLUS™超声诊断系统
K号: K160559 · 2016-10-18
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器械摘要
常见问题
What is the NOBLUS™ Ultrasound Diagnostic System?
NOBLUS™ Ultrasound Diagnostic System is a medical device that received FDA 510(k) clearance on 2016-10-18. The listed applicant is Hitachi Medical Corporation. The 510(k) number is K160559.
When did NOBLUS™ Ultrasound Diagnostic System receive FDA 510(k) clearance?
NOBLUS™ Ultrasound Diagnostic System received FDA 510(k) clearance on 2016-10-18, under 510(k) number K160559.
Who is the listed applicant for NOBLUS™ Ultrasound Diagnostic System?
The FDA 510(k) record lists Hitachi Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NOBLUS™ Ultrasound Diagnostic System?
The FDA product code for NOBLUS™ Ultrasound Diagnostic System is IYN.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
相关器械(代码:IYN)
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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